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14 results

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Page 1
Primary intradural extramedullary spinal mesenchymal chondrosarcoma: case report and literature review.
Chen CW, Chen IH, Hu MH, Lee JC, Huang HY, Hong RL, Yang SH. Chen CW, et al. BMC Musculoskelet Disord. 2019 Sep 4;20(1):408. doi: 10.1186/s12891-019-2799-2. BMC Musculoskelet Disord. 2019. PMID: 31484514 Free PMC article. Review.
BACKGROUND: Mesenchymal chondrosarcoma (MCS) is a rare malignant variant of chondrosarcoma with a high tendency of recurrence and metastasis. Intradural extramedullary spinal MCS is exceedingly rare and usually found in pediatric patients. Herein, we p …
BACKGROUND: Mesenchymal chondrosarcoma (MCS) is a rare malignant variant of chondrosarcoma with a high tendency of recu …
Sarcoma Stem Cell Heterogeneity.
Hatina J, Kripnerova M, Houfkova K, Pesta M, Kuncova J, Sana J, Slaby O, Rodríguez R. Hatina J, et al. Adv Exp Med Biol. 2019;1123:95-118. doi: 10.1007/978-3-030-11096-3_7. Adv Exp Med Biol. 2019. PMID: 31016597 Review.
The notion of this functional hierarchy operating within each tumor implies the existence of sarcoma stem cells, which may originate from mesenchymal stem cells, and indeed, mesenchymal stem cells have been used to establish several crucial experimental sarcoma mode …
The notion of this functional hierarchy operating within each tumor implies the existence of sarcoma stem cells, which may originate from …
Intracranial extra-axial mesenchymal chondrosarcoma in a 16-month-old patient with a literature review of pediatric patients.
Yapıcıer Ö, Nanah AR, Taskapılıoglu MÖ, Demir MK. Yapıcıer Ö, et al. Childs Nerv Syst. 2021 Feb;37(2):649-657. doi: 10.1007/s00381-020-04652-0. Epub 2020 May 8. Childs Nerv Syst. 2021. PMID: 32382867 Review.
Mesenchymal chondrosarcoma is a rare high-grade malignant subtype of chondrosarcoma that is characterized by undifferentiated, round, or spindled mesenchymal cells, interspersed with islands of hyaline cartilage. We report a primary intracranial extra-
Mesenchymal chondrosarcoma is a rare high-grade malignant subtype of chondrosarcoma that is characterized by undifferen
Molecular imaging of sarcomas with FDG PET.
Mendoza H, Nosov A, Pandit-Taskar N. Mendoza H, et al. Skeletal Radiol. 2023 Mar;52(3):461-475. doi: 10.1007/s00256-022-04182-7. Epub 2022 Sep 29. Skeletal Radiol. 2023. PMID: 36173459 Review.
Sarcoma comprises a heterogenous entity of musculoskeletal malignancies arising from a mesenchymal origin. The diagnosis and management of pediatric sarcoma requires a multidisciplinary approach and the use of various imaging modalities including CT, MRI and FDG PET …
Sarcoma comprises a heterogenous entity of musculoskeletal malignancies arising from a mesenchymal origin. The diagnosis and manageme …
Primary chondrosarcoma of the head and neck in pediatric patients: a clinicopathologic study of 14 cases with a review of the literature.
Gadwal SR, Fanburg-Smith JC, Gannon FH, Thompson LD. Gadwal SR, et al. Cancer. 2000 May 1;88(9):2181-8. Cancer. 2000. PMID: 10813732 Review.
BACKGROUND: Primary chondrosarcoma of the head and neck in the pediatric age group is rare. ...Follow-up was available for 11 patients; all were alive (at a mean of 14.8 years), with only a single patient demonstrating evidence of residual/ recurrent tumor (at 16.6 …
BACKGROUND: Primary chondrosarcoma of the head and neck in the pediatric age group is rare. ...Follow-up was available for 11 …
The Small Round Cell Sarcomas Complexities and Desmoplastic Presentation.
Domanski HA. Domanski HA. Acta Cytol. 2022;66(4):279-294. doi: 10.1159/000524260. Epub 2022 Apr 13. Acta Cytol. 2022. PMID: 35417916 Free PMC article. Review.
BACKGROUND: Small round cell sarcomas (SRCSs) account for most solid malignancies in the pediatric age group and are a part of group of malignant tumors characterized by heterogenous clinical presentation and overlapping microscopic features of small, round, primitive cell …
BACKGROUND: Small round cell sarcomas (SRCSs) account for most solid malignancies in the pediatric age group and are a part of group …
Sacral mesenchymal chondrosarcoma in childhood: a case report and review of the literature.
Küpeli S, Varan A, Gedikoğlu G, Büyükpamukçu M. Küpeli S, et al. Pediatr Hematol Oncol. 2010 Oct;27(7):564-73. doi: 10.3109/08880018.2010.503333. Pediatr Hematol Oncol. 2010. PMID: 20677924 Review.
Mesenchymal chondrosarcomas are rare malignant tumors in pediatric age group. ...According to the authors' literature search, the patient is the first reported case of pediatric sacral primary mesenchymal chondrosarcoma. Mesenchymal ch
Mesenchymal chondrosarcomas are rare malignant tumors in pediatric age group. ...According to the authors' literature search,
The YAP/TAZ Pathway in Osteogenesis and Bone Sarcoma Pathogenesis.
Kovar H, Bierbaumer L, Radic-Sarikas B. Kovar H, et al. Cells. 2020 Apr 15;9(4):972. doi: 10.3390/cells9040972. Cells. 2020. PMID: 32326412 Free PMC article. Review.
As the extracellular matrix composition and mechanosignaling are of particular relevance in bone formation during embryogenesis, post-natal bone elongation and bone regeneration, YAP/TAZ are believed to have critical functions in these processes. Depending on the differentiation …
As the extracellular matrix composition and mechanosignaling are of particular relevance in bone formation during embryogenesis, post-natal …
Congenital sacral mesenchymal chondrosarcoma in a neonate: a case report and review of literature.
Namini FT, Raisolsadat SM, Ghafarzadegan K, Ashkezari A. Namini FT, et al. Afr J Paediatr Surg. 2014 Jan-Mar;11(1):87-90. doi: 10.4103/0189-6725.129252. Afr J Paediatr Surg. 2014. PMID: 24647306 Review.
Mesenchymal chondrosarcomas are rare malignant tumours in children, especially, in neonates. The authors present a case of congenital mesenchymal chondrosarcoma in a 1-day neonate located in sacrum. According to the authors' literature searches, this case is
Mesenchymal chondrosarcomas are rare malignant tumours in children, especially, in neonates. The authors present a case of congenital
Intraspinal mesenchymal chondrosarcoma in a 14-year-old patient: diagnostic and therapeutic problems in relation to the review of literature.
Obuchowicz AK, Szumera-Ciećkiewicz A, Ptaszyński K, Rutynowska-Pronicka O, Madziara W, Tiszler-Cieślik E, Cieńciała M, Pietrzak J, Głowacki J, Perek D. Obuchowicz AK, et al. J Pediatr Hematol Oncol. 2012 Jul;34(5):e188-92. doi: 10.1097/MPH.0b013e318257a421. J Pediatr Hematol Oncol. 2012. PMID: 22627573 Review.
Mesenchymal chondrosarcoma (MC) is an infrequent, highly malignant neoplasm of the soft tissues and bone. It is very rare in the pediatric age group, especially in the intraspinal location. Only 24 cases have been reported to date. ...
Mesenchymal chondrosarcoma (MC) is an infrequent, highly malignant neoplasm of the soft tissues and bone. It is very rare in t
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